AU2004202612B2 - Composition formed of mercaptans which can be used in a process for the flotation of ores - Google Patents
Composition formed of mercaptans which can be used in a process for the flotation of ores Download PDFInfo
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- AU2004202612B2 AU2004202612B2 AU2004202612A AU2004202612A AU2004202612B2 AU 2004202612 B2 AU2004202612 B2 AU 2004202612B2 AU 2004202612 A AU2004202612 A AU 2004202612A AU 2004202612 A AU2004202612 A AU 2004202612A AU 2004202612 B2 AU2004202612 B2 AU 2004202612B2
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/014—Organic compounds containing phosphorus
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/008—Organic compounds containing oxygen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/012—Organic compounds containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B11/00—Obtaining noble metals
- C22B11/06—Chloridising
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2201/00—Specified effects produced by the flotation agents
- B03D2201/02—Collectors
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2203/00—Specified materials treated by the flotation agents; specified applications
- B03D2203/02—Ores
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2203/00—Specified materials treated by the flotation agents; specified applications
- B03D2203/02—Ores
- B03D2203/025—Precious metal ores
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2203/00—Specified materials treated by the flotation agents; specified applications
- B03D2203/02—Ores
- B03D2203/04—Non-sulfide ores
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B11/00—Obtaining noble metals
- C22B11/04—Obtaining noble metals by wet processes
Abstract
Composition comprising 70 - 95% of a combination of (A) n-dodecyl mercaptan (NDM) and tert-dodecyl mercaptan (TDM) in which the weight ratio NDM/TDM is 0.5-1.5, and 5 - 30% of a product (B) comprising one or aromatic or aliphatic compounds with 4-100 C and having one or two hydroxyl groups. An independent claim is also included for the process of ore recovery by flotation using the additive described.
Description
Pool Section 29 Regulation 3.2(2) AUSTRALIA Patents Act 1990 COMPLETE SPECIFICATION STANDARD PATENT Application Number: Lodged: Invention Title: Composition formed of mercaptans which can be used in a process for the flotation of ores The following statement is a full description of this invention, including the best method of performing it known to us: COMPOSITION FORMED OF MERCAPTANS WHICH CAN BE USED IN A PROCESS FOR THE FLOTATION OF ORES The present invention relates to the field of the extraction of metals and more 5 especially the flotation of ores, in particular ores based on oxides and on sulphides. It relates more particularly to a novel composition based on mercaptans which can be used, in particular, in combination with a flotation agent, and to a process for the recovery, by flotation, of metal compounds of value. Flotation is a well known process having the aim of extracting a metal from 1o low-content ores by a stage of concentration. This stage comes before a subsequent treatment comprising the heat treatment (also known as smelting) or the leaching and the refining. This is in particular the case with ores of oxides and/or of sulphides of lead, of zinc, of copper, of silver, of gold, of molybdenum and of metals belonging to the platinum group: platinum, palladium, rhodium, ruthenium, iridium and osmium. 15 The ores include the compounds (such as oxides or sulphides) of the metals to be extracted (or metal compounds of value) in the form of crystals which are dispersed in a gangue composed of various impurities, in particular siliceous impurities. The ores are therefore, after extraction from the mine, crushed and then milled in a wet medium to give particles which are sufficiently fine to release the crystals of the desired compounds. 20 During flotation, the highly heterogeneous mixture, on the one hand of the crystals of the desired compounds and, on the other hand, of the gangue particles, is therefore introduced into water comprising appropriate additives, in particular flotation agents, also known as flotation collectors. Air is injected into the aqueous suspension thus obtained, placed in a suitable device (generally a flotation cell), so as to create 25 bubbles which adhere to the crystals of the compounds (such as oxides and/or sulphides) comprising the desired metal. The adhesion of the bubbles to the said crystals is promoted by the action of the flotation agent or agents used. The crystals of the metal compounds then rise to the surface and are recovered in the form of a foam, also known as flotation concentrate. The gangue particles are recovered in the lower part of the 30 flotation cell. The flotation concentrate has a content of desired metal which is therefore considerably higher than that in the starting ore. This content depends on the initial content in the ore and on the selectivity of the flotation process. The amount of metal -2 recovered in the form of flotation concentrate for its part depends on the yield of the process. Flotation agents commonly employed in the industry for the extraction of metals include, for example, alkali metal xanthates with alkyl radicals having less than 6 5 carbon atoms, in particular potassium ethyl, amyl or isobutyl xanthate, mercapto benzothiazoles, thiocarbamates, dithiocarbamates and dithiophosphates. After a stage of drying by filtration, the flotation concentrates, for example in the case of copper, are subsequently introduced, for the heat treatment (or smelting) stage, into a furnace at temperatures which may exceed 1500*C. During this stage, the 10 desired metal is separated in the molten state from the other substances, in particular from the impurities originating from the gangue of the ore, which have to be removed in the form of a slag. It is thus understood, in particular for this reason, that it is very important on a practical level to obtain, on conclusion of the flotation stage, in addition to a high yield, a 15 concentrate which has a content of the desired metal which is as high as possible, so as to facilitate the subsequent operations of treatment of the said concentrate and of final isolation of the metal. This technical advantage for flotation concentrates with a high content of desired metal is also reflected by the enhancement in value and the cost of such concentrates, sold by mining companies to companies in charge of the recovery of 20 the metal and of its purification (or refining). This aspect of the metal content of the concentrate resulting from flotation is particularly critical in the case of platinum, the content of which in ores is extremely low and usually of the order of 2 to 15 ppm. The use of mercaptans as flotation agent is already known. French Patent Application FR 2 371 967 thus discloses the use, in the 25 production of flotation concentrates, of a solution of n-dodecyl mercaptan in a polyglycol. However, this document teaches such a use in the production of flotation concentrates with an increased content of copper. South African Patent ZA 8405787 discloses the use, as flotation collector, of a solution of tert-dodecyl mercaptan in cresylic acid. This document also discloses the 30 application of such collectors in the treatment of copper ores. In point of fact, the industry for the extraction of platinum, and more especially for the concentration of platinum ores by flotation, is, for the reasons indicated above, - 3 always looking for novel means which make it possible to improve the content of platinum in the flotation concentrates (or selectivity) and the yield of the flotation. The aim of the invention is to provide such a means, the description of which is given in the continuation of the present text. In what follows, the percentages which are 5 indicated are, in the absence of contrary indications, percentages corresponding to contents by weight. A first subject- matter of the present invention is thus a composition intended for the flotation of ores, comprising: - from 70 to 95% of a combination (A) of n-dodecyl mercaptan (or NDM) and 10 of tert-dodecyl mercaptan (or TDM), the NDM/TDM ratio by weight of which is between 0.5 and 1.5, and - from 5 to 30% of a product (B) composed of one or more aromatic or aliphatic compounds comprising from 4 to 100 carbon atoms, preferably from 5 to 40, and having one or two -OH groups. 15 This is because it has been found that this specific composition makes it possible to significantly improve the content of platinum in the filtration concentrates which are obtained from the ores by the use of conventional collecting agents and possibly the yield of the flotation operation. n-Dodecyl mercaptan is the thiol derivative of the alkyl radical comprising a 20 linear chain having 12 carbon atoms of formula n-C 12
H
25 -SH. This is a commercially available product. tert-Dodecyl mercaptan is understood to mean a mixture of compounds of formula: R-SH (I) 25 in which R is an alkyl radical having between 9 and 15 carbon atoms and having at least one tertiary carbon which is connected to the SH group. The mean number of carbon atoms in the alkyl radical is 12. The content in the mixture of the compound of formula (I) in which R is a dodecyl radical is greater than 50%, preferably greater than or equal to 60%, by weight. 30 Such a mixture is also available commercially and can be prepared by the process disclosed in Patent Application EP 0 101 356. Without being commited in any way with regard to the exact role of the product -4 (B) in the composition according to the invention, it appears that the product (B) acts as dispersing and/or foaming agent. According to a first preferred alternative form, the product (B) is chosen from the group consisting of phenols optionally substituted by one or more C 1
-C
4 alkyl 5 radicals, cresols, naphthols, xylenols, indanols and mixtures of these compounds. The said mixtures, in which the compounds are generally present in the form of their various isomers, are denoted in the present text under the term of "cresylic acid". According to another preferred alternative form, the product (B) is chosen from the group consisting of: 10 - a propylene oxide oligomer with a molecular mass of between 50 and 2000, preferably between 100 and 800; and - 2-methyl-4-pentanol, a compound also known as Methyl IsoButyl Carbinol or MIBC, of formula:
CH
3
-CH(OH)-CH
2
-CH(CH
3
)-CH
3 15 The composition according to the invention advantageously comprises from 75 to 85% of the combination (A) of NDM and TDM and from 15 to 25% of the product (B). According to a preferred alternative form, taken in combination with one of the preceding alternative forms, cresylic acid is used as product (B). 20 According to another preferred alternative form, use is made, as product (B), of MIBC or a propylene oxide oligomer with a molecular mass of between 50 and 2000, preferably between 100 and 800. According to yet another preferred alternative form, the composition according to the invention is a solution. 25 A composition according to the invention in which the NDM/TDM ratio is in the region of 1 is particularly advantageous. Another subject-matter of the present invention is a process for the recovery by flotation of metal compounds of value present in ores comprising the introduction into an appropriate cell of at least one flotation collector, characterized in that it additionally 30 comprises the introduction into the said cell of an effective amount of the composition as defined above. It is preferable to use, as flotation collector (or agent), a compound chosen from -5 alkali metal xanthates with alkyl radicals having less than 6 carbon atoms and mercaptobenzothiazoles and from thiocarbamates, dithiocarbamates and alkali metal dithiophosphates. A particularly advantageous flotation collector is an alkali metal xanthate of an 5 alkyl radical having less than 6 carbon atoms or an alkali metal dithiophosphate. It is preferable to use, as flotation agent, potassium or sodium ethyl, amyl or isobutyl xanthate. In the process according to the invention, the amount of composition based on NDM and TDM as defined above to be introduced into the process can be easily 10 determined by a person skilled in the art from preliminary tests according to various parameters, such as the content of desired metal in the ore. This amount generally corresponds to a ratio by weight, expressed on the basis of the weight of ore treated, of between 2 g/tonne and 150 g/tonne, preferably between 5 and 50 g/tonne. The ratio of the weight of the composition according to the invention to the total weight of flotation agent 15 can vary within very wide limits, for example between 0.5 and 200%, preferably between 15 and 125%. The process according to the invention may be suitable for the recovery of metal compounds, such as oxides and/or sulphides, comprising one or more metals chosen from the group consisting of: lead, zinc, copper, molybdenum, nickel, cobalt, 20 palladium, osmium, ruthenium, rhodium, iridium and platinum. The said process may also be suitable for the recovery of the said metals in the native state. However, it is preferable to employ it in the recovery of platinum compounds. The introduction of the composition according to the invention and of the flotation collector or collectors can be simultaneous or sequential. Generally, a sequential 25 introduction of the flotation collector or collectors, followed by that of the composition based on NDM and TDM according to the invention, is preferred. Finally, the composition according to the invention can be introduced both in the stage of a primary flotation and in the stage of a secondary flotation (carried out on the sterile fraction corresponding to the particles separated by settling in the lower part of 30 the cell during the primary flotation). The invention is illustrated by the following examples, which are in no way limiting.
-6 Example 1 (reference): Flotation of platinum ore with a xanthate and the dithiophosphate as flotation agents: This flotation test is carried out on a sulphide-comprising platinum ore of UG2 type originating from a South African mine in the Rustenburg region, having a platinum 5 content of 2.5 ppm. Stage 1: Preparation of an aqueous suspension of the ore by milling and sieving 1150 g of this ore are mixed with 572 g of water and introduced into a ball mill. 10 The ore is thus milled for 30 minutes. The suspension is sieved through a sieve with a mesh of 0.1 mm and an aqueous suspension A comprising 933 g of dry ore, the particles of which have a mean diameter (measured by laser particle size determination) of 40 Im, is thus recovered. 15 Stage 2: Introduction of the flotation additives into the aqueous suspension of the ore 4.5 ml of a 10.3 g/l copper sulphate solution are added to the suspension A as depressor (promoting the fall of the gangue particles in the lower part of the flotation cell). 20 Approximately 2 minutes later, 79.3 mg of sodium isobutyl xanthate and 42 mg of thiophosphate are added, these 2 products being in the form of an aqueous solution. Approximately 4 minutes later, 56 mg of cresylic acid, sold by Rttgers-Huiles Goudrons et Ddriv6s, are added. The amount of water necessary to have a total volume of 2.5 1 is added. 25 Stage 3 : Primary flotation After standing for approximately 1 minute, the mixture obtained in Stage 2 is subjected to flotation for 5 minutes at a pH in the region of 8 in a 2.5 litre laboratory cell of the Wemco type. 30 73 g of concentrate are collected by skimming off at the surface of the flotation cell. This concentrate has a platinum content of 18 ppm (corresponding to the selectivity) and includes 51.2% of the Pt present in the ore treated (the latter percentage corresponding to the yield). Stage 4 : Secondary flotation 5 The sterile fraction corresponding to the particles separated by settling in the lower part of the flotation cell is recovered and is treated with 13 mg of sodium isobutyl xanthate and 9.7 mg of sodium dithiophosphate. After mixing for 4 minutes, 5.6 mg of cresylic acid are added and the volume of water is adjusted to 2.5 1. 10 The product obtained is subjected to flotation for 3 minutes under the same conditions as in Stage 3. 26.5 g of flotation concentrate having a platinum content of 6.6 ppm, corresponding to a Pt yield of 6.8%, are recovered. The total degree of recovery of the platinum (or total yield) is therefore 58%. 15 Example 2: The following solution is prepared by simple mixing: NDM : 40% TDM : 40% 20 Cresylic acid : 20% The NDM and the TDM used are the products sold by Atofina. The cresylic acid used also originates from RUtgers-Huiles Goudrons et D6rivds. 25 Example 3: Reference Example 1 is repeated while introducing, in Stage 2, in addition to the flotation agents, 28 mg of the solution prepared in accordance with Example 2. After the primary flotation of Stage 3, 67 -g of concentrate having a platinum content of 26.6 ppm, corresponding to a yield of 66.4%, are collected. 30 The secondary flotation of Stage 4 of reference Example 1 is also repeated while adding 28 mg of the solution of Example 2. 5 g of flotation concentrate having a platinum content of 10 ppm, corresponding to a yield of 1.9%, are recovered.
The total yield is therefore 68.3%. Example 4 (reference): Flotation of platinum ore with a xanthate and the dithiophosphate as flotation agents: 5 This flotation test is carried out on a sulphide-comprising platinum ore of UG2 type originating from a South African mine in the Rustenburg region, having a platinum content of 2 ppm. Stage 1: Preparation of an aqueous suspension of the ore by milling and 10 sieving 1000 g of this ore are mixed with 508 g of water and introduced into a ball mill. The ore is thus milled for 50 minutes. The suspension is sieved through a sieve with a mesh of 0.1 mm, 20 to 30 g of ore are withdrawn for analysis and an aqueous suspension A comprising approximately 945 g of dry ore, the particles of which have a mean 15 diameter (measured by laser particle size determination) of approximately 30 pim, is thus recovered. Stage 2: Introduction of the flotation additives into the aqueous suspension of the ore 20 50 grams (expressed as equivalent per tonne of milled ore) of copper sulphate in aqueous solution are added to the suspension A in the flotation cell, stirred at 1200 rpm, as depressor (promoting the fall of the gangue particles in the lower part of the flotation cell). Approximately 2 minutes later, 85 grams (per tonne of milled ore) of sodium 25 isobutyl xanthate ard 45 grams (per tonne of milled ore) of sodium dithiophosphate are added, these two products being in the form of an aqueous solution. Approximately 4 minutes later, 60 grams (per tonne of milled ore) of a cresylic acid, comprising approximately 25% of a mixture of meta- and para-cresol, 27% of a mixture of 2,4-xylenol and 2,5-xylenol, and approximately 30% of a mixture of 30 methyl(ethyl)phenol and propyl(ethyl)phenol, are added. Such a cresylic acid is sold by Merisol. The amount of water necessary to have a total volume of 2.5 1 is added.
- 9 Stage 3 : Primary flotation After bringing the ingredients into contact for approximately 1 minute, the mixture obtained in Stage 2 is subjected to flotation for 5 minutes at a pH in the region of 8 in a 2.5 litre laboratory cell of the Wemco type. The volume of the solution is 5 maintained at 2.5 litres by addition of water throughout the duration of the flotation. The weight of concentrate collected by skimming off at the surface of the flotation cell is 124 g. The platinum content of the said concentrate (corresponding to the selectivity) is 12.2 ppm and the amount of platinum recovered (expressed as percentage of that present in the ore treated, corresponding to the yield) is 80%. 10 Example 5: Example 2 is repeated while using, as cresylic acid, that employed in Stage 2 of Example 4. 15 Example 6: The reference Example 4 is repeated while introducing, in Stage 2, in addition to the flotation agents, 30 grams (per tonne of ore) of the solution prepared in accordance with Example 5. The weight of concentrate collected is 88.7 g, for a selectivity of 14 ppm and a 20 yield of 65.9%. Example 7: Example 2 is repeated while replacing the cresylic acid by a propylene oxide oligomer with an average molecular mass of 425 sold by Bayer under the name ArcoP 25 PPG-425. Example 8: Reference Example 4 is repeated while introducing, in Stage 2, in addition to the flotation agents, 30 grams (per tonne of ore) of the solution prepared in accordance 30 with Example 7. The weight of concentrate collected is 115.6 g, for a selectivity of 12.6 ppm and a yield of 76.4%.
10 Example 9: Example 2 is repeated while replacing the cresylic acid by MIBC. Example 10: 5 Reference Example 4 is repeated by introducing, in Stage 2, in addition to the flotation agents, 30 grams (per tonne of ore) of the solution prepared in accordance with Example 9. The weight of concentrate collected is 104.8 g, for a selectivity of 12.8 ppm and a yield of 70.5%. 10 These examples show that the addition of the composition according to the invention to the flotation collectors conventionally used for the concentration of platinum significantly increases the content of platinum in the flotation concentrate and/or the yield. 15 Comprises/comprising and grammatical variations thereof when used in this specification are to be taken to specify the presence of stated features, integers, steps or components or groups thereof, but do not preclude the presence or addition of one or more other features, integers, steps, components 20 or groups thereof.
Claims (13)
1. Composition intended for the flotation of ores, comprising: - from 70 to 95% of a combination (A) of n-dodecyl mercaptan (or NDM) and 5 of tert-dodecyl mercaptan (or TDM), the NDM/TDM ratio by weight of which is between 0.5 and 1.5, and - from 5 to 30% of a product (B) composed of one or more aromatic or aliphatic compounds comprising from 4 to 100 carbon atoms, preferably from 5 to 40, and having one or two -OH groups. 10
2. Composition according to Claim 1, characterized in that the product (B) is chosen from the group consisting of phenols optionally substituted by one or more Ci-C 4 alkyl radicals, cresols, naphthols, xylenols, indanols and mixtures of these compounds. 15
3. Composition according to Claim 1, characterized in that the product (B) is chosen from the group consisting of: - a propylene oxide oligomer with a molecular mass of between 50 and 2000, preferably between 100 and 800; and - 2-methyl-4-pentanol (or MIBC). 20
4. Composition according to one of Claims 1 to 3, characterized in that it comprises from 75 to 85% of the combination (A) of NDM and TDM and from 15 to 25% of the product (B). 25
5. Composition according to one of Claims I to 4, characterized in that cresylic acid is used as product (B).
6. Composition according to one of Claims 1 to 4, characterized in that use is made, as product (B), of MIBC or a propylene oxide oligomer with a molecular mass of 30 between 50 and 2000, preferably between 100 and 800. 12
7. Composition according to any one of Claims 1 to 6, characterized in that it is a solution.
8. Composition according to any one of Claims 1 to 7, characterized in that the NDM/TDM ratio is in the region of 1. 5
9. Process for the recovery by flotation of metal compounds of value present in ores comprising the introduction into an appropriate cell of at least one flotation collector, characterized in that it additionally comprises the introduction into the said cell of an effective amount of the composition as defined in any one of Claims 1 to 8.
10 10. Process according to Claim 9, characterized in that the flotation agent is an alkali metal xanthate of an alkyl radical having less than 6 carbon atoms or an alkali metal dithiophosphate.
11. Process according to either of Claims 9 or 10, characterized in that it is employed in the recovery of platinum compounds. 15
12. A composition intended for the flotation of ores as hereinbefore described with reference to Claims 1 to 8 and with reference to the examples.
13. A process for the recovery by flotation of metal compounds of value present in ores as hereinbefore described with reference to Claims 9 to 11 and with reference to the examples. DATED this 15th day of June, 2004 ATOFINA WATERMARK PATENT & TRADE MARK ATTORNEYS 290 BURWOOD ROAD HAWTHORN VICTORIA 3122 AUSTRALIA P23234AU00
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR03.07180 | 2003-06-16 | ||
FR0307180A FR2855987B1 (en) | 2003-06-16 | 2003-06-16 | MERCAPTANS COMPOSITION FOR USE IN A FLOATING PROCESS OF ORES |
FR0403696A FR2857278B1 (en) | 2003-06-16 | 2004-04-08 | MERCAPTAN COMPOSITIONS FOR USE IN A METHOD FOR FLOATING ORES |
FR04.03696 | 2004-04-08 |
Publications (3)
Publication Number | Publication Date |
---|---|
AU2004202612A1 AU2004202612A1 (en) | 2005-01-06 |
AU2004202612B2 true AU2004202612B2 (en) | 2009-08-20 |
AU2004202612B8 AU2004202612B8 (en) | 2009-12-17 |
Family
ID=33542620
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2004202612A Active AU2004202612B8 (en) | 2003-06-16 | 2004-06-15 | Composition formed of mercaptans which can be used in a process for the flotation of ores |
Country Status (13)
Country | Link |
---|---|
US (1) | US7014048B2 (en) |
EP (1) | EP1504820B1 (en) |
CN (1) | CN100556553C (en) |
AT (1) | ATE340032T1 (en) |
AU (1) | AU2004202612B8 (en) |
CA (1) | CA2470343C (en) |
CL (1) | CL2004001496A1 (en) |
DE (1) | DE602004002439D1 (en) |
FR (1) | FR2857278B1 (en) |
MX (1) | MXPA04005870A (en) |
PE (1) | PE20050459A1 (en) |
RU (1) | RU2346751C2 (en) |
ZA (1) | ZA200404728B (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2857278B1 (en) * | 2003-06-16 | 2005-08-26 | Atofina | MERCAPTAN COMPOSITIONS FOR USE IN A METHOD FOR FLOATING ORES |
CN100551544C (en) * | 2007-02-13 | 2009-10-21 | 金堆城钼业股份有限公司 | The molybdenite foaming agent for ore dressing |
CN101264467B (en) * | 2007-03-13 | 2011-04-13 | 金堆城钼业股份有限公司 | Molybdenite and non-ferro metals floatation frother |
CN101543805B (en) * | 2008-03-28 | 2012-07-18 | 鞍钢集团矿业公司 | Chelate collector for floatation of iron mineral |
CN102806148A (en) * | 2012-09-07 | 2012-12-05 | 西北矿冶研究院 | High-sulfur copper ore collecting agent |
PE20161083A1 (en) | 2014-01-31 | 2016-11-19 | Goldcorp Inc | PROCESS FOR THE SEPARATION OF AT LEAST ONE METAL SULFIDE FROM A MIXED SULFIDE ORE OR CONCENTRATE |
US9447481B1 (en) * | 2015-10-07 | 2016-09-20 | Chevron Phillips Chemical Company Lp | Dipentene dimercaptan compositions and use thereof as a mining chemical collector |
US9512248B1 (en) | 2015-12-28 | 2016-12-06 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and use thereof as chain transfer agents |
US9505011B1 (en) | 2015-12-28 | 2016-11-29 | Chevron Phillips Chemical Company Lp | Mixed decyl mercaptans compositions and use thereof as mining chemical collectors |
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WO2000009268A1 (en) * | 1998-08-11 | 2000-02-24 | Versitech, Inc. | Flotation of sulfide mineral species with oils |
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2004
- 2004-04-08 FR FR0403696A patent/FR2857278B1/en not_active Expired - Fee Related
- 2004-06-03 AT AT04291383T patent/ATE340032T1/en not_active IP Right Cessation
- 2004-06-03 DE DE602004002439T patent/DE602004002439D1/en active Active
- 2004-06-03 EP EP04291383A patent/EP1504820B1/en active Active
- 2004-06-09 US US10/863,935 patent/US7014048B2/en active Active
- 2004-06-09 CA CA2470343A patent/CA2470343C/en active Active
- 2004-06-15 PE PE2004000593A patent/PE20050459A1/en active IP Right Grant
- 2004-06-15 RU RU2004118077/03A patent/RU2346751C2/en active
- 2004-06-15 AU AU2004202612A patent/AU2004202612B8/en active Active
- 2004-06-15 ZA ZA2004/04728A patent/ZA200404728B/en unknown
- 2004-06-15 CN CNB2004100714722A patent/CN100556553C/en active Active
- 2004-06-15 CL CL200401496A patent/CL2004001496A1/en unknown
- 2004-06-16 MX MXPA04005870A patent/MXPA04005870A/en active IP Right Grant
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FR1011166A (en) * | 1948-12-17 | 1952-06-19 | Penarroya Miniere Metall | Improvements in ore concentration by flotation |
EP0038076A1 (en) * | 1980-04-14 | 1981-10-21 | Phillips Petroleum Company | Method for removing iron impurities from glass-making sand |
US4424122A (en) * | 1982-04-19 | 1984-01-03 | Phillips Petroleum Company | Gold flotation with mercaptan and imidazoline |
US4439314A (en) * | 1982-08-09 | 1984-03-27 | Phillips Petroleum Company | Flotation reagents |
US4594151A (en) * | 1982-10-13 | 1986-06-10 | Societe Nationale Elf Aquitaine (Production) | Flotation of minerals |
WO2000009268A1 (en) * | 1998-08-11 | 2000-02-24 | Versitech, Inc. | Flotation of sulfide mineral species with oils |
Also Published As
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ATE340032T1 (en) | 2006-10-15 |
AU2004202612B8 (en) | 2009-12-17 |
CL2004001496A1 (en) | 2005-02-25 |
DE602004002439D1 (en) | 2006-11-02 |
FR2857278B1 (en) | 2005-08-26 |
CN100556553C (en) | 2009-11-04 |
AU2004202612A1 (en) | 2005-01-06 |
PE20050459A1 (en) | 2005-08-25 |
MXPA04005870A (en) | 2005-06-08 |
FR2857278A1 (en) | 2005-01-14 |
CA2470343A1 (en) | 2004-12-16 |
EP1504820A1 (en) | 2005-02-09 |
CN1575854A (en) | 2005-02-09 |
RU2346751C2 (en) | 2009-02-20 |
US20050167339A1 (en) | 2005-08-04 |
ZA200404728B (en) | 2005-04-26 |
EP1504820B1 (en) | 2006-09-20 |
RU2004118077A (en) | 2006-02-27 |
US7014048B2 (en) | 2006-03-21 |
CA2470343C (en) | 2011-01-25 |
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